ENST00000327669.5:c.*2670T>G
MANE Select
|
ENSP00000328347.4:n.*2670T>G
|
|
ENST00000327669.4:c.3636T>G
|
ENSP00000328347.4:n.3636T>G
|
|
NM_001077710.2:c.*2670T>G
|
NP_001071178.2:n.*2670T>G
|
|
XM_011510372.1:c.*2696T>G
|
XP_011508674.1:n.*2696T>G
|
|
XM_011510373.1:c.*2696T>G
|
XP_011508675.1:n.*2696T>G
|
|
XM_011510374.1:c.*2696T>G
|
XP_011508676.1:n.*2696T>G
|
|
XM_011510372.2:c.*2696T>G
|
XP_011508674.1:n.*2696T>G
|
|
XM_017004691.1:c.*2729T>G
|
XP_016860180.1:n.*2729T>G
|
|
XR_001738890.1:n.4169T>G
|
|
|
NM_001077710.3:c.*2670T>G
MANE Select
|
NP_001071178.2:n.*2670T>G
|
|